[0001] The present invention relates to single crystal silicon typically for use as a substrate
of semiconductor integrated circuits. More particularly, the invention is directed
to such single crystal silicon in which contamination with certain specific impurities
is minimized in the bulk of the substrate so that stacking faults induced on main
or front surfaces during thermal oxidation are reduced substantially to zero.
[0002] Thermal oxidation is commonly accepted as requisite of processing integrated circuits,
particularly those of an MOS type. Oxygen-induced stacking faults referred to simply
as OSF and developed while in treatment of single crystal silicon at elevated temperature
are found significantly contributive to the electrical characteristics of the integrated
circuit to be formed. OSF, therefore, has heretofore been a great concern in the electronics
industry.
[0003] OSF is generally known to grow in an oxidative atmosphere and to reduce under a non-oxidative
condition. This type of fault is reportedly attributable to (a) mechanical strains
induced during wafer fabrication, (b) point defects developed and accumulated in heat
processing, (c) defects due to ion implantation. (d) surface contaminations with Na,
and (e) surface defects such as so-called swirl defects and bulk defects originating
from dissolved oxygen deposition.
[0004] The surface and bulk defects among those factors are closely associated with various
IG treatments effected initially in the production of integrated circuits from silicon
wafers. The IG treatments are effective to prevent the wafer from getting involved
in OSF as they are capable of rendering the wafer fully free from oxygen-induced minute
defects at the active surface layer. It has been further proposed, as taught for instance
by Japanese Patent Laid-open Publication No. 55-56098, that oxygen-induced bulk defects
in the bulk of single crystal silicon be prohibited by controlling the thermal history
of single crystal silicon during the period of time when the latter material is being
pulled by Czochralski method. This prior process is intended to subject a rod of
single crystal silicon just following the whole growth process in a temperature region
of 900 to 500°C in the furnace chamber for not longer than 4 hours and thereafter
at a cooling speed of not lower than 100°C per hour.
[0005] The surface and bulk defects would also be expected to result from contamination
with metallic impurities. To this end, many attempts have been made to examine and
detect those contaminants introduced in single crystal silicon, as disclosed in the
following publications. However, none of them make a detailed analysis of the correlation
between the individual metals and the OSF levels.
1. P. T. Schmit et al, "Solid-state Science and Technology", J. Electrochem. Soc.,
p.632 (1981)
2. Nakajima and Ohara, "Chemical Analyses of Semiconductors", 0hyô Butsuri, Vol.
43, No. 5, p.438 (1974)
3. Nakajima, Bando and Nakayama, "Neutron Activation Analyses of Impurities in Highly
Pure Silicon Semiconductors", Bunseki Kiki, Vol. 6, No. 9, p572 (1968)
4. Shirai, "Pulling Technology of Single Crystal Silicons", Zairyo Gijutsu, Vol. 2,
No. 1, p.41 (1984)
[0006] Neutron activation analysis allows a limited group of metals such as Au to be detected
in the order of ppta but fails to measure various other metals up to such level of
concentration.
[0007] Under the above state of technologies, there has been left unsolved the technical
problem of OSF being held at a substantially nil level in single crystal silicon.
[0008] The present invention seeks to provide single crystal silicon for use as a substrate
of semiconductor integrated circuits which exhibits lesser susceptibility to OSF on
a semiconducting substrate and has an OSF density of not more than 10 or 100 pieces/cm²
for an n-type, (100)-orientation semiconducting substrate.
[0009] The single crystal silicon according to the present invention, because of its minimum
generation of OSF, is favorably applicable to the production of various semiconductor
devices of superior electrical characteristics.
[0010] According to one aspect of the invention, there is provided single crystal silicon
for use as a substrate of semiconductor integrated circuits having n-type conductivity
with the polished (100) orientation front surface, comprising as impurities Cu, Fe,
Ni, and Cr in an individual concentration of not more than 0.1 ppta and in a total
content of not more than 0.4 ppta, whereby the silicon has minimized generation of
oxygen-induced stacking faults.
[0011] According to another aspect of the invention, there is provided single crystal silicon
for use as a substrate of semiconductor integrated circuits having n-type conductivity
with the polished (100) orientation front surface, comprising as impurities Cu, Fe,
Ni, Cr, Ti and Mn in an individual concentration of not more than 0.1 ppta and in
a total content of not more than 0.6 ppta, whereby the silicon has minimized generation
of oxygen-induced stacking faults.
[0012] Single crystal silicon according to the present invention is suitable for the production
of various semiconductor devices of superior electrical characteristics. A first
form of single crystal silicon contemplated under the invention comprises metallic
contaminants in which are included Cu, Fe, Ni and Cr. Each of the contaminants should
not be greater than 0.1 ppta in concentration, whereas all these contaminants should
be smaller than 0.4 ppta in total content. By strict observance of these requirements,
the OSF density is maintained at below 100 pieces/cm² as an n-type semiconductor
substrate (100)-oriented and mirror-polished.
[0013] A second form of silicon is so structured as to have an OSF density of less than
10 pieces/cm². In such instance, metallic impurities are Cu, Fe, Ni, Cr, Ti and Mn,
respectively, in a concentration of not more than 0.1 ppta and, on the whole, in a
content of not more than 0.6 ppta. To attain OSF densities up to 100 pieces/cm², Ti
and Mn if excessively present are not likely to involve anything adverse.
[0014] A certain method of analysis has previously been developed by the present inventor
so as to detect metallic contaminants introduced in single crystal silicon during
the pulling stage by the Czochralski (CZ) method. This analysis method is conspicuously
superior in accuracy to conventional counterparts, as described in Japanese Patent
Application No. 1-82840. Impurities, i.e. Cu, Fe, Ni, Cr, Ti and Mn, are determinable
with the limits of detection in the order of 0.01 ppta; that is, a residual melt in
a quartz crucible is examined at a solidification ratio of single crystal silicon
grown in the CZ method in which polycrystalline silicon is molten with heat in the
crucible, followed by immersion into the melt and pull of seed crystal therefrom and
by subsequently continuous growth of single crystal rod. The invention is based upon
the finding where correlations between the contents of individual impurities in single
crystal pulled and the densities of OSF on the substrate processed therefrom were
made clear by taking advantage of such high accuracy analysis.
[0015] Several publications disclose, only in part, that metal contamination causes OSF
generation in single crystal silicon resulting from crystal growth by the pulling
method. The silicon thus grown is known to lead to nucleation of minute defects due
chiefly to the defects of lattice and to the presence of dissolved oxygen. This latter
oxygen when in a super-saturated state develops minute defects and when carbon dissolved
those defects increase over the level without dissolved carbon. It is to be recognized
in the art that nucleation of minute defects will be caused also by metallic contaminants
for reasons noted in connection with the behavior of oxygen.
[0016] It has now been found that OSF densities can be selectively reduced to 100 pieces/cm²
and to 10 pieces/cm² by the limitation of selected metals in specified concentrations
and contents.
[0017] The invention will be further described by way of the following examples which should
be construed as illus trative rather than restrictive.
Examples 1 to 6 and Comparative Examples 1 to 4
[0018] Into a quarts crucible of 45 cm in diameter was charged 60 kg of polycrystalline
silicon which was thereafter doped with phosphorus and molten with heat. An n-type,
(100)-orientation, 155-cm diameter rod of single crystal silicon was pulled from the
melt.
[0019] Impurity concentration in the single crystal silicon was quantitated by determining
the concentrations of the various impurities in the crucible residue. The silicon
melt was solidified, after pulling of the single crystal silicon, to the residue of
about 100 g. The resulting residue melt was fully solidified by cooling, followed
by comminution and cleaning on the surface and by subsequent dissolution in an aqueous
mixture of hydrofluoric acid an nitric acid. Measurement of impurity concentrations
was then made in accordance with ICP from which the concentrations of contaminants
in the single crystal silicon were converted by the following equation.
C = C₀.k(1-X)
k-1
where C : impurity concentration in single silicon,
C₀: impurity concentration in initial charge,
k : diffusion coefficient, and
X : solidification ratio.
[0020] As the parameter k, a value is used which is reported in W. Zulenhner et al, "Silicon
Chemical Etching", Crystal, Vol 8, p.28. In general, heavy metal contaminants are
extremely small in k, say about 10⁻⁶, and hence likely to remain in almost all amounts
in a residual melt without appreciable inclusion on silicon crystals. It is therefore
sufficient to analyze the residual melt in determining the initial concentrations
of contaminants as C₀. The ratio of solidification is zero at an initial stage. This
is taken to mean that the foregoing equation may be rearranged to C = C₀.k. More specifically,
the impurity concentration in single crystal silicon is defined as [impurity concentration
in residual melt x silicon weight of residual melt (100 g)/crystalline silicon weight
(60 kg)] x k.
[0021] The results obtained are shown in Table 1 along with the quantitative lower limits.
Metals contained in the melt have been proved to be primarily Cu, Fe, Ni, Cr, Ti and
Mn. Table 2 represents the quantitative lower limits of those six metals in single
crystal silicon.
Table 2
Element |
Lower limit (ppta) |
Ti |
0.0005 |
Cr |
0.0001 |
Mn |
0.00002 |
Fe |
0.0001 |
Ni |
0.001 |
Cu |
0.02 |
[0022] Different single crystal silicon rods were prepared to have varied concentrations
of the primary metals as shown in Table 3. On pulling at an overall length of 110
cm, each of the test silicon rods was sliced at an interval of 10 cm to wafers of
0.075 mm in thickness each for each. Mirror polishing, steam oxidation at 1,150°C
in a furnace, cooling to room temperature and removal of oxide film with aqueous hydrofluoric
acid solution from the sample surface were done in that order. After etching by immersion
into a selective etching solution for 2 minutes, the developed OSF density on the
etched surface was examined on an optical microscope.
[0023] Cu, Fe, Ni and Cr when reduced to the specified contents prevent OSF development
as evidenced by Table 3. Ti and Mo have turned out, even with increased contents,
not to invite increased OSF.
Table 3
Impurity concentration (ppta) |
Examples |
|
1 |
2 |
3 |
4 |
Cu |
0.1 |
0.05 |
0.05 |
0.05 |
Fe |
0.05 |
0.12 |
0.05 |
0.05 |
Ni |
0.05 |
0.05 |
0.06 |
0.05 |
Cr |
0.05 |
0.05 |
0.05 |
0.1 |
Ti |
0.3 |
0.3 |
0.3 |
0.3 |
Mn |
0.2 |
0.2 |
0.2 |
0.2 |
OSF density (pieces/cm²) |
80 |
50 |
75 |
50 |
[0024] Controls, comparative Examples 1 to 4, were prepared as shown in Table 4 and treated
as in Examples 1 to 4.
[0025] Either one of Cu, Fe, Ni and Cr when exceeding the specified amounts reveals a sharp
rise in OSF.
Table 4
Impurity concentration (ppta) |
Comparative Examples |
|
1 |
2 |
3 |
4 |
Cu |
0.2 |
0.05 |
0.05 |
0.05 |
Fe |
0.05 |
0.2 |
0.05 |
0.05 |
Ni |
0.05 |
0.05 |
0.1 |
0.05 |
Cr |
0.05 |
0.05 |
0.05 |
0.2 |
Ti |
0.3 |
0.3 |
0.3 |
0.3 |
Mn |
0.2 |
0.2 |
0.2 |
0.2 |
OSF density (pieces/cm²) |
400 |
300 |
300 |
250 |
[0026] As has been confirmed from Table 5, Ti and Mn when set within the specified amounts,
together with Cu, Fe, Ni and Cr, OSF is significantly reduced. This is particularly
true of Example 6 in which all these metals are present at 0.05 ppta. OSF is nil.
Table 5
Impurity concentration (ppta) |
Examples |
|
5 |
6 |
Cu |
0.05 |
0.05 |
Fe |
0.05 |
0.05 |
Ni |
0.05 |
0.05 |
Cr |
0.05 |
0.05 |
Ti |
0.14 |
0.05 |
Mn |
0.1 |
0.05 |
OSF density (pieces/cm²) |
20 |
0 |